Christian Wentzel

581 total citations
8 papers, 373 citations indexed

About

Christian Wentzel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christian Wentzel has authored 8 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christian Wentzel's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Christian Wentzel is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Christian Wentzel collaborates with scholars based in Sweden, Switzerland and Ireland. Christian Wentzel's co-authors include Ann‐Charlotte Thuresson, Göran Annerén, Maria Fernström, Parri Wentzel, Jonas Cederberg, C. Martin Simán, Lisa Borg, Ulf J. Eriksson, Eva‐Lena Stattin and Lars Feuk and has published in prestigious journals such as Journal of Lipid Research, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Christian Wentzel

8 papers receiving 347 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Christian Wentzel Sweden	7	196	188	112	64	52	8	373
Altuğ Koç Türkiye	11	107 0.5×	157 0.8×	80 0.7×	44 0.7×	14 0.3×	53	356
Ricardo Gracía Spain	11	277 1.4×	241 1.3×	64 0.6×	50 0.8×	16 0.3×	17	461
Frédérique Tihy Canada	11	120 0.6×	215 1.1×	146 1.3×	30 0.5×	8 0.2×	18	384
Ying Peng China	11	185 0.9×	215 1.1×	160 1.4×	41 0.6×	8 0.2×	44	500
Yvonne Arens Netherlands	14	122 0.6×	110 0.6×	127 1.1×	36 0.6×	19 0.4×	22	428
Chantal Gendrot France	11	82 0.4×	91 0.5×	23 0.2×	68 1.1×	25 0.5×	15	301
Vicki Mattern United States	10	110 0.6×	43 0.2×	109 1.0×	27 0.4×	36 0.7×	18	302
Nidhi Shah United States	12	96 0.5×	136 0.7×	59 0.5×	23 0.4×	30 0.6×	40	339
Winnie Courtens Belgium	16	256 1.3×	431 2.3×	158 1.4×	86 1.3×	5 0.1×	29	587
Josep Calafell-Segura Spain	16	130 0.7×	67 0.4×	163 1.5×	25 0.4×	11 0.2×	32	563

Countries citing papers authored by Christian Wentzel

Since Specialization

Citations

This map shows the geographic impact of Christian Wentzel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christian Wentzel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christian Wentzel more than expected).

Fields of papers citing papers by Christian Wentzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christian Wentzel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christian Wentzel. The network helps show where Christian Wentzel may publish in the future.

Co-authorship network of co-authors of Christian Wentzel

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Wentzel. A scholar is included among the top collaborators of Christian Wentzel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christian Wentzel. Christian Wentzel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

Hülsmeier, Andreas J., Sandra P. Toelle, Peter Bellstedt, et al.. (2023). The atypical sphingolipid SPB 18:1(14Z);O2 is a biomarker for DEGS1 related hypomyelinating leukodystrophy. Journal of Lipid Research. 64(12). 100464–100464. 6 indexed citations

Halvardson, Jonatan, Jin Zhao, Ammar Zaghlool, et al.. (2016). Mutations in HECW2 are associated with intellectual disability and epilepsy. Journal of Medical Genetics. 53(10). 697–704. 48 indexed citations

Wentzel, Christian, Göran Annerén, & Ann‐Charlotte Thuresson. (2014). A maternal de novo non-reciprocal translocation results in a 6q13-q16 deletion in one offspring and a 6q13-q16 duplication in another. European Journal of Medical Genetics. 57(6). 259–263. 16 indexed citations

Wentzel, Christian, Evica Rajcan‐Separovic, Claudia Ruivenkamp, et al.. (2011). Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11. European Journal of Human Genetics. 19(9). 959–964. 27 indexed citations

Wentzel, Christian, Sally Ann Lynch, Eva‐Lena Stattin, et al.. (2010). Interstitial Deletions at 6q14.1–q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype. Molecular Syndromology. 1(2). 75–81. 25 indexed citations

Wentzel, Christian, et al.. (2008). Clinical variability of the 22q11.2 duplication syndrome. European Journal of Medical Genetics. 51(6). 501–510. 125 indexed citations

Wentzel, Parri, et al.. (2001). Induction of embryonic dysmorphogenesis by high glucose concentration, disturbed inositol metabolism, and inhibited protein kinase C activity. Teratology. 63(5). 193–201. 60 indexed citations

Eriksson, Ulf J., Lisa Borg, Jonas Cederberg, et al.. (2000). Pathogenesis of Diabetes-Induced Congenital Malformations. Upsala Journal of Medical Sciences. 105(2). 53–84. 66 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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